[1] Fretzayas A, Moustaki M, Liapi O, et al. Gilbert syndrome. Eur J Pediatrics, 2012,171:11-15. [2] Horsfall LJ, Nazareth I, Pereira SP, et al. Gilbert’s syndrome and the risk of death:a population-based cohort study. Gastroenterol Hepatol, 2013,28:1643-1647. [3] Gilbert A, Lereboullet P. La cholamae simple familiale. Sem Med, 1901,21:241-248. [4] Hirschfieid GM, Alexander JG. Gilbert syndrome:an overview for clinical biochemists. Ann Clin Biochem, 2006,43:340-343. [5] Canu G,Minucci A,Zuppi C, et al. Gilbert and Crigler Najjar syndromes:an update of the UDP-Glucuronosyltransferase1A1(UGT1A1) gene mutation databaseclinical.Blood Cells Mol Dis, 2013,50:273-280. [6] 孙梅,谈国蕾,王建芳,等. 家族性胆红素异常患者UGT1A1基因检测及其基因多态性分析.肝脏,2017,22:15-19. [7] Monaghan G, Mclellan A, Mcgeehan A, et al. Gilbert’s syndrome is a contributory factor in prolonged unconjugated hyperbilirubinemia of the newborn. Pediatr, 1999,134:441-446. [8] Kitsiou-Tzeli S, Kanavakis E, Tzetis M, et al. Gilbert’s syndrome as a predisposing factor for idiopathic cholelithiasis in children. Haematologica,2003,88:1193-1194. [9] Tsezou A, Tzetis M, Giannatou E, et al. Gilbert syndrome as a predisposing factor for cholelithiasis risk in the Greek adult population.Genet Test Mol Biomark, 2009,13:143-146. [10] Hussien E, Sara Y, Mohamed S, et al. Gilbert’s syndrome as a cause of unconjugated hyperbilirubinemia after living donor liver transplantation.transplant international, 2015,28:563. [11] Strassburg CP, Hyperbilirunemia syndromes (Gilbert-Meulengracht,Grigler-Najjar, Dubin-Johnson and Rotor syndrome).Best Pract Res Clin Gastroenterol, 2010, 24:555-571. [12] 江小柯,范竹萍. Gilbert综合征与药物代谢.国际消化病杂志,2012,12: 339-341. |